Interfacial design for lithium–sulfur batteries: From liquid to solid

IF 22.2 Q1 CHEMISTRY, MULTIDISCIPLINARY EnergyChem Pub Date : 2019-07-01 DOI:10.1016/j.enchem.2019.100002
Min Yan , Wen-Peng Wang , Ya-Xia Yin , Li-Jun Wan , Yu-Guo Guo
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引用次数: 95

Abstract

Li–S batteries, offering high theoretical energy density of 2600 Wh kg−1, low cost and nontoxicity, are considered as a fascinating next-generation electric energy storage devices. However, the dissolution of the lithium polysulfides (LiPSs), shuttle effect and safety issues of Li anode notoriously pose great challenges for the commercialization of Li–S batteries. These problems derive from the interfacial issues among cathodes, separators, electrolytes and anodes, which in turn can be resolved by rational interface tailoring. This review mainly focuses on these interfacial issues in Li–S batteries with traditional liquid electrolytes and the latest research trend including gel polymer electrolytes, solid polymer electrolytes, solid inorganic electrolytes and hybrid electrolytes. In the liquid electrolyte systems, sulfur cathodes can effectively avoid severe shuttle effects and maintain stable cycling with the interfacial regulations of coatings, freestanding interlayers and separator modifications, while Li anode can be modified by protective layers, functional additives, three-dimensional current collectors and Li alloys. In quasi-solid systems (gel polymer electrolytes and hybrid electrolytes), rational designs are applied considering the utility of active materials, restraining LiPSs and suppressing Li dendrites. In all solid-state electrolyte systems (solid polymer electrolytes and solid inorganic electrolytes), the emphasis is to enhance the ionic conductivities and reduce the interfacial resistances. Mechanisms underlying these interfacial issues and corresponding electrochemical performances are discussed. Recent developments on the interfacial designs of Li–S batteries are summarized and highlighted. Based on the most critical factors of the interfaces proposed, prospectives are presented to pave the avenue for the designs of Li–S batteries.

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锂硫电池的界面设计:从液体到固体
Li-S电池理论能量密度高达2600 Wh kg - 1,成本低,无毒,被认为是下一代电能存储设备的理想选择。然而,锂多硫化物(LiPSs)的溶解、锂阳极的穿梭效应和安全性问题给锂电池的商业化带来了巨大挑战。这些问题源于阴极、隔膜、电解质和阳极之间的界面问题,而这些问题又可以通过合理的界面裁剪来解决。本文主要综述了传统液体电解质和凝胶聚合物电解质、固体聚合物电解质、固体无机电解质和混合电解质等Li-S电池中存在的这些界面问题。在液体电解质体系中,硫阴极可以通过涂层、独立夹层和分离器的界面调节来有效避免剧烈的穿梭效应,保持稳定的循环,而锂阳极可以通过保护层、功能添加剂、三维集流器和锂合金来改性。在准固体体系(凝胶聚合物电解质和杂化电解质)中,考虑到活性材料的效用,合理设计,抑制LiPSs和抑制Li枝晶。在所有固态电解质体系(固体聚合物电解质和固体无机电解质)中,重点是提高离子电导率和降低界面电阻。讨论了这些界面问题的机制和相应的电化学性能。综述了锂硫电池界面设计的最新进展。基于所提出的接口的最关键因素,提出了为锂硫电池设计铺平道路的前景。
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来源期刊
EnergyChem
EnergyChem Multiple-
CiteScore
40.80
自引率
2.80%
发文量
23
审稿时长
40 days
期刊介绍: EnergyChem, a reputable journal, focuses on publishing high-quality research and review articles within the realm of chemistry, chemical engineering, and materials science with a specific emphasis on energy applications. The priority areas covered by the journal include:Solar energy,Energy harvesting devices,Fuel cells,Hydrogen energy,Bioenergy and biofuels,Batteries,Supercapacitors,Electrocatalysis and photocatalysis,Energy storage and energy conversion,Carbon capture and storage
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